Introducing the RAPAFLO® Promise

The RAPAFLO® Promise

RAPAFLO Promise Seal

Watson is committed to producing products that help patients live better. If RAPAFLO® does not meet your patients' needs, we will reimburse up to a $50 copay for the first time the patient uses another prescription treatment (terazosin, doxazosin, tamsulosin, or alfuzosin).

Who is eligible?

  • Patients who are new to therapy with RAPAFLO®
    • Patients who have paid for 1 month of RAPAFLO® therapy and used it as prescribed
  • Patients may have taken another prescription treatment prior to beginning RAPAFLO® therapy

How does the RAPAFLO® Promise work?

  • Patient complies with 1 month of paid RAPAFLO® treatment
  • Within 60 days of filling the prescription of the competitive product, patient sends the documentation required as described in the patient information leaflet provided by your RAPAFLO® representative:
    • Acknowledgment that 1) patient is not receiving copay assistance or free medication for the new product prescription; 2) patient is not enrolled in Medicare, Medicaid, TriCare, or any other state or federal healthcare program; and 3) patient is not a resident of Massachusetts, Rhode Island, or anywhere else prohibited by law
    • Proof of purchase of 1-month of RAPAFLO® therapy and a 1 month supply of competitor’s product as described above

Terms and Conditions

  • Patients must be new to therapy with RAPAFLO® but could have previously taken a competing product prior to beginning RAPAFLO® therapy
  • Patients receiving copay assistance for RAPAFLO® are eligible
  • Patients must provide proof of 1 paid month of therapy with RAPAFLO®, proof of purchase of competing product, and the card attached to the patient information leaflet
  • Offer expires 60 days after the date the prescription for the competitive product (terazosin, doxazosin, tamsulosin, or alfuzosin) is filled at the pharmacy
  • Patients cannot be receiving copay assistance or free product from manufacturer of competing product
  • Total patient reimbursement is limited to $50 or actual out-of-pocket cost, whichever is lower
  • Watson reserves the right to rescind, revoke, or amend this offer without notice at any time
  • Watson will not sell or rent patient’s personal information to others
  • This offer is not valid for individuals who are covered on Medicaid, Medicare, TriCare, or any other state or federal healthcare program
  • Not valid for residents of Massachusetts, Rhode Island, or anywhere else prohibited by law
  • Offer good only in the United States and Puerto Rico
References
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  2. RAPAFLO® (silodosin) Capsules full Prescribing Information, November 2009.
  3. Marks LS, Gittelman MC, Hill LA, Volinn W, Hoel G. Rapid efficacy of the highly selective α1A-adrenoceptor antagonist silodosin in men with signs and symptoms of benign prostatic hyperplasia: pooled results of 2 phase 3 studies. J Urol. 2009;181:2634-2640.
  4. National Institute of Diabetes and Digestive and Kidney Diseases. Prostate enlargement: benign prostatic hyperplasia. NIH Publication No. 07-3012. June 2006.
  5. Bruskewitz RC. Quality of life and sexual function in patients with benign prostatic hyperplasia. Rev Urol. 2003;5:72-80.
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  9. Data on file, Watson Laboratories, Inc.
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  13. Fagelman E, Lowe FC. Herbal medications in the treatment of benign prostatic hyperplasia (BPH). Urol Clin N Am. 2002;29:23-29, vii.
  14. National Institute on Aging: Talking With Your Doctor: A Guide For Older People. NIH Publication No. 05-3452. August 2005 (Reprinted April 2010). Available at: http://www.nia.nih.gov/NR/rdonlyres/90DF996C-DF5F-4245-B7CA-B2E1B993D8C7/0/TWYD_0521_web.pdf. Accessed July 29, 2010.
  15. Medline Plus Medical Encyclopedia from NIH: Enlarged Prostate. Available at: http://www.nlm.nih.gov/medlineplus/ency/article/000381.htm. Accessed July 29, 2010.
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  17. Kuritzky L. A primary care physician’s perspective on benign prostatic hyperplasia. Rev Urol. 2003;5(suppl 5):S42-S48.
  18. Wolters R, et al: Lower urinary tract symptoms: social influence is more important than symptoms in seeking medical care. BJU Int. 2002;90:655–661.
  19. Rosen RC, Giuliano F, Cason CC. Sexual dysfunction and lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH). Eur Urol. 2005;47:824–837.
  20. Ponholzer A, Madersbacher S. Lower urinary tract symptoms and erectile dysfunction; links for diagnosis, management and treatment. Int J Impot Res. 2007;19:544-550.
  21. MacDiarmid SA, Hill LA, Volinn W, Hoel G. Lack of pharmacodynamic interaction of silodosin, a highly selective α1a-adrenoceptor antagonist, with the phosphodiesterase-5 inhibitors sildenafil and tadalafil in healthy men. Urology. 2010;75:520-525.
  22. Marks LS. Reply to editorial comment. Urology. 2009;74:1323-1324.
  23. Schwinn DA, Roehrborn CG. α1-Adrenoceptor subtypes and lower urinary tract symptoms. Int J Urol. 2008;15:193-199.
  24. Straus SM, Kors JA, De Bruin ML, et al. Prolonged QTc interval and risk of sudden cardiac death in a population of older adults. J Am Coll Cardiol. 2006;47:362-367.
  25. Carbone DJ, Hodges S. Medical therapy for benign prostatic hyperplasia: sexual dysfunction and impact on quality of life. Int J Impot Res. 2003;15:299-306.
  26. Nomiya M, Yamaguchi O. A quantitative analysis of mRNA expression of alpha 1 and beta-adrenoceptor subtypes and their functional roles in human normal and obstructed bladders. J Urol. 2003;170(2 Pt 1):649-653.
  27. Murata S, Taniguchi T, Takahashi M, et al. Tissue selectivity of KMD-3213, an α1-adrenoreceptor antagonist, in human prostate and vasculature. J Urol. 2000;164:578-583.
  28. Stafford-Smith M, Bartz R, Wilson K, et al. Alpha-adrenergic mRNA subtype expression in the human nasal turbinate. Can J Anesth. 2007;54:549-555.
  29. Wei JT, Calhoun E, Jacobsen SJ. Urologic Diseases in America Project: benign prostatic hyperplasia. J Urol. 2008;179(5 Suppl.):S75-S80.
  30. Issa MM, Regan T. Medical therapy for benign prostatic hyperplasia—present and future impact. Am J Manag Care. 2007;13:S4-S9.
  31. Berry SJ, Coffey DS, Walsh PC, et al. The development of human benign prostatic hyperplasia with age. J Urol. 1984;132:474.
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RAPAFLO® is indicated for the treatment of the signs and symptoms of benign prostatic hyperplasia (BPH). RAPAFLO® is not indicated for the treatment of hypertension.

Important Safety Information

RAPAFLO® is contraindicated in patients with severe renal impairment (CCr <30 mL/min), severe hepatic impairment (Child-Pugh score ≥10), and with use of strong CYP3A4 inhibitors. Postural hypotension with or without symptoms (eg, dizziness) may develop when beginning treatment with RAPAFLO®. As with all alpha-blockers, there is a potential for syncope. Patients should be warned of the possible occurrences of such events and should avoid situations where injury could result. RAPAFLO® should be used with caution in patients with moderate renal impairment. Patients should be assessed to rule out the presence of prostate cancer prior to starting treatment with RAPAFLO®. Patients planning cataract surgery should inform their ophthalmologist that they are taking RAPAFLO®.

The most common side effects are retrograde ejaculation, dizziness, diarrhea, orthostatic hypotension, headache, nasopharyngitis, and nasal congestion.